GENETIC ENCYCLOPEDIA
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GRCh37/hg19 Xp22.2(chrX:9910182-9935526)x2 AND not provided

Significance: Benign
ClinVar: RCV000753376

Variant: GRCh37/hg19 Xp22.2(chrX:9910182-9935526)x2

Type: Variant
Allele: GRCh37/hg19 Xp22.2(chrX:9910182-9935526)x2 608076
Gene:
Type: copy number gain
Location: ChrX: 9910182 - 9935526 - assembly GRCh37

Condition

Disease: not provided